Počet záznamov: 1
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder
- Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder / Liskova P., Ulmanova O. ... [et al.]. -- Popis urobený z citácie a doplnený z databázy PubMed
In Acta ophthalmologica. -- Vol. 91, no. 3 (2013), s. e225-e231
I. Líšková, Petra
II. Ulmanová, Olga
III. Acta ophthalmologica. -- Vol. 91, no. 3 (2013), s. e225-e231
Počet záznamov: 1